Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 5
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 3
rs4820599
LRRC75B ; GGT1
0.925 0.160 22 24594246 intron variant A/G snv 0.43 3
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 2
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 1